Hnia Karim, Zouiten Dora, Cantel Sonia, Chazalette Delphine, Hugon Gérald, Fehrentz Jean-Alain, Masmoudi Ahmed, Diment Ann, Bramham Janice, Mornet Dominique, Winder Steve J
Université Montpellier 1, Unité de Formation et de Recherche de Médecine, Laboratoire de Physiologie des Interactions, Institut de Biologie, Boulevard Henri IV, F-34062, France.
Biochem J. 2007 Feb 1;401(3):667-77. doi: 10.1042/BJ20061051.
Dystrophin forms part of a vital link between actin cytoskeleton and extracellular matrix via the transmembrane adhesion receptor dystroglycan. Dystrophin and its autosomal homologue utrophin interact with beta-dystroglycan via their highly conserved C-terminal cysteine-rich regions, comprising the WW domain (protein-protein interaction domain containing two conserved tryptophan residues), EF hand and ZZ domains. The EF hand region stabilizes the WW domain providing the main interaction site between dystrophin or utrophin and dystroglycan. The ZZ domain, containing a predicted zinc finger motif, stabilizes the WW and EF hand domains and strengthens the overall interaction between dystrophin or utrophin and beta-dystroglycan. Using bacterially expressed ZZ domain, we demonstrate a conformational effect of zinc binding to the ZZ domain, and identify two zinc-binding regions within the ZZ domain by SPOTs overlay assays. Epitope mapping of the dystrophin ZZ domain was carried out with new monoclonal antibodies by ELISA, overlay assay and immunohistochemistry. One monoclonal antibody defined a discrete region of the ZZ domain that interacts with beta-dystroglycan. The epitope was localized to the conformationally sensitive second zinc-binding site in the ZZ domain. Our results suggest that residues 3326-3332 of dystrophin form a crucial part of the contact region between dystrophin and beta-dystroglycan and provide new insight into ZZ domain organization and function.
肌营养不良蛋白通过跨膜黏附受体肌营养不良聚糖,构成肌动蛋白细胞骨架与细胞外基质之间重要连接的一部分。肌营养不良蛋白及其常染色体同源物抗肌萎缩蛋白聚糖,通过其高度保守的富含半胱氨酸的C末端区域与β - 肌营养不良聚糖相互作用,该区域包括WW结构域(含有两个保守色氨酸残基的蛋白质 - 蛋白质相互作用结构域)、EF手型结构域和ZZ结构域。EF手型结构域稳定WW结构域,提供肌营养不良蛋白或抗肌萎缩蛋白聚糖与肌营养不良聚糖之间的主要相互作用位点。ZZ结构域含有一个预测的锌指基序,稳定WW和EF手型结构域,并加强肌营养不良蛋白或抗肌萎缩蛋白聚糖与β - 肌营养不良聚糖之间的整体相互作用。利用细菌表达的ZZ结构域,我们证明了锌与ZZ结构域结合的构象效应,并通过斑点印迹分析确定了ZZ结构域内的两个锌结合区域。通过ELISA、印迹分析和免疫组织化学,用新的单克隆抗体对肌营养不良蛋白ZZ结构域进行了表位作图。一种单克隆抗体确定了ZZ结构域中与β - 肌营养不良聚糖相互作用的离散区域。该表位定位于ZZ结构域中对构象敏感的第二个锌结合位点。我们的结果表明,肌营养不良蛋白的3326 - 3332位残基形成了肌营养不良蛋白与β - 肌营养不良聚糖之间接触区域的关键部分,并为ZZ结构域的组织和功能提供了新的见解。